Natalie Rogers (Czmola), CCRA

Senior Clinical Trial Manager at Advanced Clinical
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Pittsburgh, Pennsylvania, United States, US
Languages
  • Ukrainian -

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

You need to have a working account to view this content.
Join now
You need to have a working account to view this content.
Join now

Credentials

  • Certified Clinical Research Associate
    Association of Clinical Research Professionals
    Oct, 2015
    - Nov, 2024

Experience

  • Advanced Clinical
    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Senior Clinical Trial Manager
      • Mar 2023 - Present

    • Clinical Trial Manager
      • Aug 2021 - Apr 2023

  • PPD
    • United States
    • Research Services
    • 700 & Above Employee
    • Clinical Team Manager
      • Aug 2020 - Aug 2021

  • Novum Pharmaceutical Research Services
    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Lead Clinical Research Associate
      • Mar 2017 - Aug 2020

    • Clinical Research Associate II
      • Jun 2016 - Mar 2017

  • Atlantic Research Group
    • United States
    • Biotechnology
    • 1 - 100 Employee
    • Clinical Research Associate II
      • Oct 2015 - Jun 2016

    • Clinical Research Associate
      • Mar 2015 - Sep 2015

  • Novum Pharmaceutical Research Services
    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Clinical Research Associate
      • Apr 2014 - Feb 2015

      Acquire therapeutic knowledge pertinent to each protocol Conduct on-site pre-study site selection, site initiation, monitoring, and close-out visits Managing multiple sites across multiple protocols throughout the United States 100% Source to CRF verification Ensure adherence to FDA regulations and ICH/GCP guidelines Review drug accountability records and ensure drug accountability accuracy on-site Travel ~80% Weekly site status tracking Manage report writing, letters… Show more Acquire therapeutic knowledge pertinent to each protocol Conduct on-site pre-study site selection, site initiation, monitoring, and close-out visits Managing multiple sites across multiple protocols throughout the United States 100% Source to CRF verification Ensure adherence to FDA regulations and ICH/GCP guidelines Review drug accountability records and ensure drug accountability accuracy on-site Travel ~80% Weekly site status tracking Manage report writing, letters, and travel expenses in a timely manner Verify regulatory compliance on site Trained Evaluator assisting in the training of new employees

    • Clinical Research Specialist
      • Jul 2013 - Apr 2014

Education

  • University of Pittsburgh at Greensburg
    B.A., Biology
    2007 - 2012

Community

You need to have a working account to view this content. Click here to join now